メチルテストステロン

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H350：発がんのおそれ

• 注意書き

  P201：使用前に取扱説明書を入手すること。

  P202：全ての安全注意を読み理解するまで取り扱わないこ と。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P308+P313：暴露または暴露の懸念がある場合：医師の診断/手当てを 受けること。

  P405：施錠して保管すること。

  P501：内容物/容器を．．．に廃棄すること。

メチルテストステロン 価格

MSDS Information

• 17-Methyltestosterone

メチルテストステロン 化学特性,用途語,生産方法

• 外観

  白色～わずかにうすい黄色、結晶性粉末～粉末

• 溶解性

  エタノール(95)及びメタノールに溶けやすく、アセトンにやや溶けやすく、水にほとんど溶けない。

• 用途

  薬理研究用。

• 用途

  合成テストステロンです。黄 体ホルモン依存性の腫瘍増殖抑制作用を示し ます。

• 効能

  男性ホルモン補充薬, アンドロゲン受容体作動薬

• 使用上の注意

  アルゴン封入

• 説明

  Methyltestosterone is a synthetic analog of testosterone that possesses all of the properties of testosterone, exhibiting stimulatory action on the development of male sex organs and secondary sex characteristics, although it is not degraded by enzymes in the gastrointestinal tract, and therefore it can only be taken orally

• 化学的特性

  white to slightly yellowish-white crystalline

• 使用

  Androgen. It has been used as an androgenic agent. Controlled substance (anabolic steroid).

• 定義

  ChEBI: A 17beta-hydroxy steroid that is testosterone bearing a methyl group at the 17alpha position.

• 薬物動態学

  The synthesis of 17α-methyltestosterone made available a compound that was orally active in daily doses between 10 and 50 mg, which is equivalent to a 400 mg oral dose of testosterone. The presence of a 17α alkyl group reduces susceptibility to hepatic oxidative metabolism, thereby increasing oral bioavailability by slowing metabolism. Following oral administration, methyltestosterone is well absorbed from the gastrointestinal tract, with a half-life of approximately 3 hours. This drug has the androgenic and anabolic activities of testosterone. Although orally active, it is more effective when administered sublingually. The alkylated oral androgens should be viewed as potentially hepatotoxic and should not be used.

• 安全性プロファイル

  Poison by intraperitoneal route. Moderately toxic by ingestion. Human teratogenic effects by ingestion: developmental abnormalities of the urogenital system. Experimental teratogenic and reproductive effects. Human systemic effects: cholestatic jaundce, weight loss or decreased weight gain. Questionable human carcinogen producing liver tumors. A synthetic androgenic steroid. When heated to decomposition it emits acrid smoke and irritating fumes.

• 純化方法

  This anabolic steroid is crystallised from hexane or hexane/*benzene. It has E1cm 1% 495-530 at 241nm (EtOH). The colour reaction with 2,4-dinitrophenyl hydrazine is used for assaying it. [Gornall & Macdonald J Biol Chem 201 279 1953.] In another colour reaction the sterone (1mg) in acetic acid (0.2ml) + 88% H3PO4 (2mL) is allowed to stand for 1hour when it becames fluorescent. After 1hour it is diluted with acetic acid (~3mL) and provides a strong yellow fluorescence with the intensity of 50-100 times that of estrone. [Stuart & Stuckey J Pharm Pharmacol 1 130 1949, Openauer Rec Trav Chim Pays-Bas 56 137 137, Beilstein 8 IV 1010.]

メチルテストステロン 上流と下流の製品情報

メチルテストステロン 生産企業

Global(358)Suppliers

メチルテストステロン スペクトルデータ(¹HNMR、¹³CNMR、IR1、IR2、MS)

58-18-4, メチルテストステロン キーワード